Neurofibromatosis-1: Genetic disorder often leading to tumors on nerves.
More detailed information about the symptoms,
causes, and treatments of Neurofibromatosis-1 is available below.
Symptoms of Neurofibromatosis-1
See full list of 22
symptoms of Neurofibromatosis-1
Treatments for Neurofibromatosis-1
Read more about treatments for Neurofibromatosis-1
Home Diagnostic Testing
Home medical testing related to Neurofibromatosis-1:
- Colon & Rectal Cancer: Home Testing
Wrongly Diagnosed with Neurofibromatosis-1?
Review possible medical complications related to Neurofibromatosis-1:
Causes of Neurofibromatosis-1
Read more about causes of Neurofibromatosis-1.
Disease Topics Related To Neurofibromatosis-1
Research the causes of these diseases that are similar to, or related to, Neurofibromatosis-1:
Neurofibromatosis-1: Undiagnosed Conditions
Commonly undiagnosed diseases in related medical categories:
Misdiagnosis and Neurofibromatosis-1
Undiagnosed stroke leads to misdiagnosed aphasia: BBC News UK reported on a man who
had been institutionalized and treated for mental illness
because he suffered from sudden inability to speak.
This was initially misdiagnosed as a ...read more »
Dementia may be a drug interaction: A common scenario in aged care is for
a patient to show mental decline to dementia.
Whereas this can, of course, occur due to various...read more »
Spitz nevi misdiagnosed as dangerous melanoma skin cancer: One possible misdiagnosis to
consider in lieu of melanoma is spitz nevi.
See melanoma and...read more »
Mild traumatic brain injury often remains undiagnosed: Although the symptoms
of severe brain injury are hard to miss,
it is less clear for milder injuries, or even those causing a...read more »
MTBI misdiagnosed as balance problem: When a person has symptoms
such as vertigo or dizziness, a diagnosis of brain injury may go overlooked.
This is particularly true of mild traumatic brain injury...read more »
Psoriasis often undiagnosed cause of skin symptoms in children: Children who suffer
from the skin disorder called psoriasis can often go undiagnosed.
The main problem is that psoriasis is rare in children, and not often
seen by...read more »
Brain pressure condition often misdiagnosed as dementia: A condition
that results from an excessive pressure of CSF within the brain is often...read more »
Post-concussive brain injury often misdiagnosed: A study found that soldiers who had
suffered a concussive injury in battle often were misdiagnosed on their return.
A variety of symptoms can occur in post...read more »
Children with migraine often misdiagnosed: A migraine often fails to be
correctly diagnosed in pediatric patients.
These patients are not the typical migraine...read more »
Vitamin B12 deficiency under-diagnosed: The condition of Vitamin B12 deficiency
is a possible misdiagnosis of various conditions, such as multiple sclerosis (see symptoms of multiple sclerosis).
See symptoms of Vitamin B12...read more »
Read more about Misdiagnosis and Neurofibromatosis-1
Neurofibromatosis-1: Research Doctors & Specialists
Research related physicians and medical specialists:
- Bone, Joint and Orthopedic Specialists:
- Nerve Specialists:
- Cancer Specialists:
- Neurology (Brain/CNS Specialists):
- more specialists...»
Other doctor, physician and specialist research services:
Hospitals & Clinics: Neurofibromatosis-1
Research quality ratings and patient safety measures
for medical facilities in specialties related to Neurofibromatosis-1:
Hospital & Clinic quality ratings »
Choosing the Best Hospital:
More general information, not necessarily in relation to Neurofibromatosis-1,
on hospital performance and surgical care quality:
Neurofibromatosis-1: Rare Types
Rare types of diseases and disorders in related medical categories:
More Neurofibromatosis-1 animations & videos
Prognosis for Neurofibromatosis-1
Prognosis for Neurofibromatosis-1:
NF1 is usually mild, though it can sometimes be severe.
More about prognosis of Neurofibromatosis-1
Research about Neurofibromatosis-1
Visit our research pages for current research about Neurofibromatosis-1 treatments.
Clinical Trials for Neurofibromatosis-1
The US based website ClinicalTrials.gov lists information on both federally
and privately supported clinical trials using human volunteers.
Some of the clinical trials listed on ClinicalTrials.gov for Neurofibromatosis-1 include:
See full list of 12
Clinical Trials for Neurofibromatosis-1
Statistics for Neurofibromatosis-1
Neurofibromatosis-1: Broader Related Topics
Types of Neurofibromatosis-1
Neurofibromatosis-1 Message Boards
Related forums and medical stories:
User Interactive Forums
Read about other experiences, ask a question about Neurofibromatosis-1, or answer someone else's question, on our message boards:
Definitions of Neurofibromatosis-1:
Type 1 (peripheral) neurofibromatosis (von Recklinghausen's disease), is the most common type of neurofibromatosis. It is characterized clinically by cutaneous and subcutaneous tumors with patches of hyperpigmentation. The hyperpigmented skin areas, are present from birth and found anywhere on the body surface. They can vary markedly in size and color. The dark brown areas are called cafe-au-lait spots. The multiple cutaneous and subcutaneous tumors are nerve sheath neoplasms, called neurofibromas. They can develop anywhere along the peripheral nerve fibers. Neurofibromas can become quite large, causing a major disfigurement, eroding bone, and compressing various peripheral nerve structures. Type 1 neurofibromatosis has dominant inheritance, with a gene locus on the proximal long arm of chromosome 17. -- 2003
- (Source - Diseases Database)
Neurofibromatosis-1 is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Neurofibromatosis-1, or a subtype of Neurofibromatosis-1,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Neurofibromatosis-1 as a "rare disease".
Source - Orphanet
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